Table 1.
names—family common (latin binomial) | region | population | abundance metric | years | pre-1992 slopea | post-1992 slopea | change in abundanceb | Amat | Lmat | growth | age-structure | citationc |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Rajidae | ||||||||||||
barndoor skate (Dipturus laevis) | NWA | E Scotian Shelf | CPUETOT | 1958–2001 | −0.020 | 0.000 | D | 0 | 0 | 0 | 0 | 1 |
W Scotian Shelf | CPUETOT | 1962–2003 | −0.010 | 0.011 | D | 0 | 0 | 0 | 0 | 1 | ||
NMA | Georges Bank | BTOT | 1986–2001 | −0.160 | 0.289 | I | 0 | 0 | 0 | 0 | 1 | |
thorny skate (Amblyraja radiata) | NWA | Grand Banks | SSB | 1980–2002 | −0.043 | 0.054 | D | 0 | 0 | 0 | 0 | 2 |
West Greenland | CPUETOT | 1982–2002 | −0.112 | −0.051 | D | 0 | 0 | 0 | 0 | 3 | ||
Macrouridae | ||||||||||||
roughhead grenadier (Macrourus berlgax) | NWA | Labrador, Newfoundland, Grand Banks | BTOT | 1978–1995 | −0.100 | 0.015d | ? | 0 | 0 | 0 | 0 | 4 |
roundnose grenadier (Coryphaenoides rupsestris) | NEA | Subareas IV, VI, VII | BTOT | 1996–2003 | — | −0.154 | D | 0 | 0 | 1 | 0 | 5 |
Phycidae | ||||||||||||
white hake (Urophycis tenuis) | NWA | Grand Banks | BTOT | 1972–2001 | 0.020 | 0.258d | ? | 0 | 0 | 0 | 0 | 6 |
S Gulf of St Lawrence (4T) | BTOT | 1971–2000 | 0.023 | 0.014 | D | 0 | 0 | 1 | 1 | 7 | ||
Scotian Shelf (4VWX/5) | NSSB | 1970–2001 | 0.019 | −0.071 | D | 0 | 0 | 0 | 1 | 8 | ||
NMA | Georges Bank, Gulf of Maine | CPUETOT | 1963–2001 | 0.016 | −0.078 | S | 0 | 0 | 0 | 0 | 9 | |
Merlucciidae | ||||||||||||
hake (Merluccius merluccius) | NEA | northern stock | SSB | 1978–2003 | −0.047 | 0.008 | D | 0 | 0 | 1 | 1 | 5 |
southern stock | SSB | 1982–2003 | −0.099 | −0.031 | D | 0 | 0 | 1 | 1 | 5 | ||
Pacific hake (M. productus) | NEP | Canada & US | SSB | 1988–1998 | −0.104 | −0.109 | D | 0 | 0 | 1 | 1 | 10 |
silver hake (M. bilinearis) | NWA | Scotian Shelf | CPUETOT | 1970–2003 | 0.007 | −0.049 | D | 1 | 1 | 1 | 1 | 11 |
Gadidae | ||||||||||||
Atlantic cod (Gadus morhua) | NEA | Baltic (22–24) | SSB | 1970–2004 | −0.049 | −0.003 | D | 1 | 0 | 1 | 1 | 12 |
Baltic (25–32) | SSB | 1966–2003 | 0.010 | −0.044 | D | 1 | 0 | 1 | 1 | 5, 12 | ||
Celtic Sea (Div. VIIe–k) | SSB | 1971–2003 | 0.035 | −0.034 | I | 0 | 0 | 1 | 1 | 5 | ||
Faroe Bank | CPUETOT | 1983–2003 | −0.204 | 0.285 | I | 0 | 0 | 0 | 0 | 12 | ||
Faroe Plateau | SSB | 1961–2004 | −0.013 | 0.022 | S | 1 | 0 | 1 | 1 | 12 | ||
Iceland | SSB | 1955–2004 | −0.048 | 0.024 | D | 1 | 0 | 1 | 1 | 12 | ||
Irish Sea | SSB | 1968–2003 | −0.019 | −0.070 | D | 1 | 0 | 1 | 1 | 5 | ||
Kattegat | SSB | 1971–2004 | −0.061 | −0.200 | D | 1 | 0 | 1 | 1 | 12 | ||
NE Arctic | SSB | 1946–2004 | −0.020 | −0.028 | D | 1 | 1 | 1 | 1 | 12, 13 | ||
North Sea | SSB | 1963–2003 | −0.037 | −0.057 | D | 0 | 0 | 1 | 1 | 5 | ||
Norway coast | SSB | 1984–2001 | 0.000 | −0.145 | D | 1 | 0 | 0 | 1 | 12 | ||
West of Scotland | SSB | 1978–2003 | −0.061 | −0.186 | D | 0 | 0 | 1 | 1 | 5 | ||
NWA | Cabot Strait (4Vn) | SSB | 1981–2000 | −0.135 | −0.027 | D | 0 | 0 | 1 | 1 | 14 | |
E Scotian Shelf (4VsW) | SSB | 1970–2002 | 0.023 | −0.140 | D | 1 | 1 | 1 | 1 | 15 | ||
E Georges Bank | SSB | 1978–2003 | −0.021 | −0.013 | D | 0 | 0 | 1 | 1 | 16 | ||
Flemish Cap (3M) | SSB | 1988–2002 | 0.068 | −0.300 | D | 1 | 0 | 1 | 1 | 17, 18 | ||
Greenland offshore | NSSB | 1982–2003 | −0.134 | 0.268 | D | 0 | 0 | 1 | 1 | 12 | ||
N Gulf of St Lawrence (3Pn4RS) | SSB | 1974–2003 | −0.064 | 0.030 | D | 1 | 0 | 1 | 1 | 19 | ||
Northern cod (2J3KL) | SSB | 1962–2002 | −0.081 | −0.099 | D | 1 | 1 | 1 | 1 | 14, 20 | ||
S Grand Banks (3NO) | SSB | 1959–2003 | −0.061 | −0.101 | D | 1 | 0 | 1 | 1 | 21 | ||
S Gulf of St Lawrence (4T) | SSB | 1950–2003 | 0.004 | −0.027 | D | 0 | 0 | 1 | 1 | 22 | ||
St Pierre Bank (3Ps) | SSB | 1959–2001 | −0.018 | 0.007 | D | 1 | 0 | 1 | 1 | 23 | ||
W Scotian Shelf (4X) | SSB | 1970–2002 | −0.014 | −0.055 | D | 0 | 0 | 1 | 1 | 24 | ||
NMA | Georges Bank | SSB | 1978–2001 | −0.041 | −0.010 | D | 1 | 1 | 1 | 1 | 9, 25, 26 | |
Gulf of Maine | SSB | 1982–2001 | −0.003 | 0.032 | D | 1 | 1 | 1 | 1 | 9, 25, 26 | ||
blue ling (Molva dypterygia) | NEA | Iceland | CPUETOT | 1985–2003 | 0.002 | −0.059 | D | 0 | 0 | 0 | 0 | 12 |
cusk/torsk (Brosme brosme) | NEA | Iceland | CPUESSB | 1986–2003 | −0.062 | −0.043 | D | 0 | 0 | 0 | 0 | 12 |
NWA | Scotia–Fundy | CPUETOT | 1970–2001 | −0.035 | −0.001 | D | 0 | 0 | 0 | 0 | 27, 28 | |
haddock (Melanogrammus aeglefinus) | NEA | Faroe | SSB | 1961–2003 | 0.001 | 0.132 | I | 1 | 0 | 1 | 1 | 5, 12 |
Iceland | SSB | 1979–2004 | −0.037 | 0.047 | D | 1 | 0 | 1 | 1 | 12 | ||
NE Arctic | SSB | 1950–2004 | −0.021 | −0.008 | D | 1 | 0 | 1 | 1 | 5, 12 | ||
North Sea & Skagarrek | SSB | 1963–2003 | −0.050 | 0.064 | D | 0 | 0 | 1 | 1 | 5 | ||
West of Scotland | SSB | 1978–2003 | −0.049 | −0.001 | S | 0 | 0 | 1 | 1 | 5 | ||
NWA | S Gulf & E Scotian Shelf (4TVW) | SSB | 1970–2000 | 0.026 | 0.108 | D | 1 | 1 | 1 | 1 | 29, 30 | |
W Scotian Shelf & Gulf of Maine | SSB | 1970–2003 | −0.022 | 0.073 | D | 0 | 0 | 1 | 1 | 31 | ||
E Georges Bank (5Zc) | SSB | 1969–2003 | −0.001 | 0.167 | D | 0 | 0 | 1 | 1 | 32 | ||
NMA | Georges Bank | SSB | 1963–2001 | −0.067 | 0.210 | D | 0 | 0 | 1 | 1 | 9 | |
Gulf of Maine | CPUETOT | 1963–2001 | −0.135 | 0.520 | D | 0 | 0 | 0 | 0 | 9 | ||
ling (Molva molva) | NEA | Iceland | CPUETOT | 1985–2003 | −0.067 | −0.023 | D | 0 | 0 | 1 | 1 | 12 |
Pacific cod (Gadus macrocephalus) | NEP | W coast Vancouver Island | BTOT | 1988–2002 | −0.375 | −0.083 | D | 0 | 0 | 0 | 0 | 33 |
Hecate Strait | BTOT | 1956–2001 | 0.007 | −0.123 | D | 0 | 0 | 0 | 0 | 34 | ||
pollock/saithe (Pollachias virens) | NEA | Faroe | SSB | 1961–2004 | −0.016 | 0.057 | I | 1 | 0 | 1 | 1 | 12 |
Iceland | SSB | 1962–2004 | −0.007 | −0.026 | I | 1 | 0 | 1 | 1 | 12 | ||
NE Arctic | SSB | 1960–2004 | −0.056 | 0.117 | I | 0 | 0 | 1 | 1 | 12 | ||
North Sea (IV), VI, IIIa | SSB | 1967–2002 | −0.052 | 0.097 | D | 0 | 0 | 1 | 1 | 5 | ||
NWA | E Georges Bank & Scotian shelf | SSB | 1982–1999 | −0.042 | 0.041 | D | 0 | 0 | 1 | 1 | 35 | |
NMA | Georges Bank, Gulf of Maine | SSB | 1963–2001 | −0.038 | 0.119 | I | 0 | 0 | 0 | 0 | 9 | |
whiting (Merlangius merlangus) | NEA | Celtic Sea | SSB | 1982–2003 | 0.058 | −0.016 | I | 0 | 0 | 1 | 1 | 5 |
Irish Sea | SSB | 1980–2002 | −0.08 | −0.262 | D | 0 | 0 | 1 | 1 | 5 | ||
North Sea (IV) & VIId | SSB | 1980–2002 | −0.046 | −0.031 | D | 0 | 0 | 1 | 1 | 5 | ||
West of Scotland | SSB | 1978–2003 | −0.070 | −0.096 | D | 0 | 0 | 1 | 1 | 5 | ||
Lophiidae | ||||||||||||
anglerfish/monkfish (Lophius americanus) | NWA | E Georges Bank & Scotian shelf | CPUETOT | 1970–2000 | −0.061 | 0.055 | D | 0 | 0 | 0 | 0 | 36 |
W Grand Banks | BTOT | 1977–2000 | 0.064 | 0.117d | ? | 0 | 0 | 0 | 0 | 37, 38 | ||
anglerfish (L. budegassa) | NEA | Divisions VIIb–k, VIIIa,b | SSB | 1986–2003 | −0.035 | −0.002 | D | 0 | 0 | 1 | 1 | 5 |
anglerfish (L. piscatorius) | NEA | Divisions VIIb–k, VIIIa,b | SSB | 1986–2003 | −0.080 | 0.004 | D | 0 | 0 | 1 | 1 | 5 |
Scorpaenidae | ||||||||||||
Acadian redfish (Sebastes fasciatus) | NMA | Georges Bank, Gulf of Maine | CPUETOT | 1963–2001 | −0.066 | 0.177 | S | 0 | 0 | 0 | 0 | 9 |
bocaccio (S. paucispinis) | NEP | BC | CPUETOT | 1980–2001 | −0.081 | −0.146 | D | 0 | 0 | 0 | 0 | 39 |
redfish (S. marinus) | NEA | East Greenland | CPUETOT | 1985–2003 | −0.292 | 0.252 | D | 0 | 0 | 0 | 0 | 12 |
Iceland | CPUESSB | 1985–2003 | −0.082 | 0.052 | D | 0 | 0 | 0 | 0 | 12 | ||
Subareas I, II | CPUESSB | 1992–2003 | – | −0.131 | D | 0 | 0 | 0 | 1 | 12 | ||
redfish (S. mentella, S. fasciatus) | NWA | Gulf of St Lawrence | CPUETOT | 1992–2000 | – | −0.169 | D | 0 | 0 | 0 | 0 | 40 |
Flemish Cap | CPUESSB | 1979–2002 | −0.120 | −0.032 | D | 1 | 1 | 1 | 1 | 41 | ||
SW Grand Banks | CPUETOT | 1992–2000 | – | 0.067 | S | 0 | 0 | 0 | 0 | 42, 43 | ||
redfish (S. mentella, S. marinus) | NWA | W Greenland inshore | CPUESSB | 1982–2002 | −0.327 | −0.053 | D | 0 | 0 | 0 | 0 | 44 |
redfish (S. mentella, S. fasciatus, S. marinus) | NWA | Labrador & E Newfoundland | CPUETOT | 1978–2000 | −0.208 | 0.055 | D | 0 | 0 | 0 | 0 | 45 |
Anoplopomatidae | ||||||||||||
sablefish (Anoplopoma fimbria) | NEP | British Columbia | CPUETOT | 1992–2003 | — | −0.144 | D | 0 | 0 | 0 | 0 | 46 |
Zoarcidae | ||||||||||||
ocean pout (Zoarces americanus) Anarhichadidae | NMA | Cape Cod-Delaware | CPUETOT | 1968–2002 | 0.006 | −0.008 | D | 0 | 0 | 0 | 0 | 9 |
northern wolffish (Anarhichus denticulatus) | NWA | Labrador, Newfoundland, Grand Banks | CPUETOT | 1981–2001 | −0.209 | 0.001 | D | 0 | 0 | 0 | 0 | 47 |
spotted wolffish (A. minor) | NWA | Labrador, Newfoundland, Grand Banks | CPUETOT | 1981–2001 | −0.207 | 0.146 | D | 0 | 0 | 0 | 0 | 47 |
W Greenland | CPUESSB | 1982–2002 | −0.224 | 0.150 | D | 0 | 0 | 0 | 0 | 3 | ||
striped wolffish (A. lupus) | NWA | Labrador, Newfoundland, Grand Banks | CPUETOT | 1977–2001 | −0.190 | 0.152 | D | 0 | 0 | 0 | 0 | 47 |
W Greenland | CPUESSB | 1982–2002 | −0.211 | 0.022 | D | 0 | 0 | 0 | 0 | 3 | ||
Ammodytidae | ||||||||||||
sandeel (Ammodytes spp.) | NEA | North Sea | SSB | 1983–2003 | −0.097 | −0.044 | D | 0 | 0 | 1 | 1 | 5 |
Scophthalmidae | ||||||||||||
megrim (Lepidorhombus boscii) | NEA | Spain & Portugal (VIIIc, IXa) | SSB | 1986–2003 | −0.003 | 0.013 | D | 0 | 0 | 1 | 1 | 5 |
megrim (L. whiffagonis) | NEA | Divisions VII, VIIIa,b,d | SSB | 1984–2003 | −0.055 | 0.023 | D | 0 | 0 | 1 | 1 | 5 |
Spain & Portugal (VIIIc, IXa) | SSB | 1986–2003 | −0.046 | 0.012 | D | 0 | 0 | 1 | 1 | 5 | ||
windowpane (Scophthalmus aquosus) | NMA | Georges Bank, Gulf of Maine | CPUETOT | 1963–2001 | 0.033 | 0.094 | I | 0 | 0 | 0 | 0 | 9 |
S New England & mid-Atlantic Bight | CPUETOT | 1963–2001 | −0.043 | 0.082 | D | 0 | 0 | 0 | 0 | 9 | ||
Paralichthyidae (Paralichthys dentatus) | NMA | U.S. | SSB | 1982–2002 | −0.126 | 0.157 | I | 0 | 0 | 1 | 1 | 60 |
Pleuronectidae | ||||||||||||
American plaice (Hippoglossoides platessoides) | NWA | W Greenland | SSB | 1983–2002 | −0.295 | −0.073 | D | 0 | 0 | 0 | 0 | 3 |
Labrador & Newfoundland (2J3K) | SSB | 1979–2003 | −0.085 | −0.048 | D | 1 | 1 | 0 | 1 | 48 | ||
Grand Banks (3LNO) | CPUESSB | 1984–2002 | −0.189 | −0.017 | D | 1 | 1 | 1 | 1 | 49 | ||
Flemish Cap (3M) | CPUETOT | 1988–2002 | −0.156 | 0.000 | D | 0 | 0 | 1 | 1 | 50 | ||
St Pierre Bank (3Ps) | CPUESSB | 1983–2002 | −0.175 | 0.065 | D | 1 | 1 | 1 | 1 | 51 | ||
S Gulf of St Lawrence | CPUESSB | 1967–1999 | −0.06 | 0.043 | D | 0 | 0 | 1 | 1 | 52 | ||
Scotian Shelf (4VW) | BTOT | 1970–2000 | −0.025 | 0.000 | D | 0 | 1 | 1 | 0 | 53 | ||
NMA | Georges Bank, Gulf of Maine | SSB | 1980–2000 | −0.138 | 0.025 | D | 1 | 0 | 1 | 1 | 9 | |
flounder (Platichthyes flesus) | NEA | Baltic (24&25) | SSB | 1978–2003 | −0.024 | −0.016 | S | 1 | 0 | 1 | 1 | 12 |
Greenland halibut (Reinhardtius hipploglossoides) | NEA | Iceland | CPUESSB | 1996–2003 | — | 0.079 | S | 0 | 0 | 0 | 0 | 5 |
NE Arctic | SSB | 1964–2004 | −0.058 | 0.054 | D | 1 | 0 | 1 | 1 | 12 | ||
NWA | Gulf of St Lawrence | CPUETOT | 1992–2002 | — | 0.046 | I | 1 | 0 | 0 | 0 | 54 | |
Labrador, Newfoundland, Grand Banks (2J3KL) | CPUETOT | 1978–2002 | −0.003 | 0.021 | D | 0 | 0 | 0 | 1 | 55, 56 | ||
W Greenland | SSB | 1987–2002 | 0.104 | 0.003 | I | 0 | 0 | 1 | 1 | 57,58 | ||
plaice (Pleuronectes platessa) | NEA | Celtic Sea | SSB | 1977–2003 | 0.070 | −0.053 | I | 0 | 0 | 1 | 1 | 5 |
Eastern Channel | SSB | 1980–2003 | 0.058 | −0.007 | S | 0 | 0 | 1 | 1 | 5 | ||
Irish Sea | SSB | 1964–2003 | −0.018 | −0.010 | D | 0 | 0 | 1 | 1 | 5 | ||
Kattegat & Skaggerak | SSB | 1978–2003 | −0.021 | 0.033 | S | 0 | 0 | 1 | 1 | 5 | ||
North Sea | SSB | 1957–2003 | −0.002 | −0.039 | D | 1 | 1 | 1 | 1 | 5, 59 | ||
Western Channel | SSB | 1976–2003 | 0.063 | −0.019 | I | 0 | 0 | 1 | 1 | 5 | ||
winter flounder (Pseudopleuronectes americanus) | NWA | S Gulf of St. Lawrence | CPUETOT | 1972–2001 | 0.003 | −0.001 | I | 0 | 0 | 1 | 0 | 61 |
NMA | Georges Bank | BTOT | 1964–2001 | −0.039 | 0.174 | S | 0 | 0 | 0 | 0 | 9 | |
S New England & mid-Atlantic Bight | SSB | 1981–2001 | −0.129 | 0.090 | D | 0 | 0 | 0 | 1 | 9 | ||
witch flounder (Glyptocephalus cynoglossus) | NWA | Labrador & Newfoundland | BTOT | 1984–2002 | −0.241 | −0.004 | D | 0 | 0 | 0 | 0 | 62 |
S Grand Banks | CPUETOT | 1984–2002 | −0.119 | 0.026 | D | 0 | 0 | 0 | 0 | 63 | ||
St. Pierre Bank | BTOT | 1983–2001 | 0.035 | 0.029 | D | 0 | 0 | 1 | 1 | 64 | ||
Gulf of St. Lawrence | CPUETOT | 1987–2000 | −0.183 | 0.097 | D | 0 | 0 | 0 | 1 | 65 | ||
NMA | Gulf of Maine & Georges Bank | SSB | 1982–2001 | −0.125 | 0.000 | D | 0 | 0 | 1 | 1 | 9 | |
yellowtail flounder (Limanda ferruginea) | NWA | E Scotian Shelf (4VW) | BTOT | 1986–2000 | −0.273 | 0.090 | D | 0 | 0 | 0 | 0 | 53 |
Grand Banks (3LNO) | CPUETOT | 1984–2002 | −0.120 | 0.179 | S | 1 | 1 | 0 | 1 | 66, 67 | ||
S Gulf of St. Lawrence | CPUETOT | 1971–2001 | 0.038 | −0.001 | I | 0 | 0 | 0 | 0 | 68 | ||
NMA | Georges Bank | SSB | 1973–2003 | −0.104 | 0.200 | I | 0 | 0 | 1 | 1 | 69 | |
Gulf of Maine & Cape Cod | SSB | 1985–2001 | 0.225 | 0.008 | I | 0 | 0 | 1 | 1 | 70 | ||
S New England & mid-Atlantic Bight | SSB | 1973–2001 | −0.035 | 0.101 | D | 0 | 0 | 1 | 1 | 9, 71 | ||
Soleidae | ||||||||||||
sole (Solea solea) | NEA | Bay of Biscay | SSB | 1984–2003 | −0.002 | −0.053 | D | 0 | 0 | 1 | 1 | 5 |
Celtic Sea | SSB | 1971–2003 | −0.037 | 0.026 | D | 0 | 0 | 1 | 1 | 5 | ||
Eastern Channel | SSB | 1982–2003 | 0.013 | −0.017 | I | 0 | 0 | 1 | 1 | 5 | ||
Irish Sea | SSB | 1970–2003 | −0.009 | 0.002 | D | 0 | 0 | 1 | 1 | 5 | ||
North Sea | SSB | 1957–2003 | −0.016 | −0.076 | D | 0 | 0 | 1 | 1 | 5 | ||
Skaggerak & Kattegak | SSB | 1984–2004 | 0.180 | −0.126 | I | 0 | 0 | 1 | 1 | 12 | ||
Western Channel | SSB | 1969–2003 | 0.010 | −0.027 | D | 0 | 0 | 1 | 1 | 5 |
Trends in abundance are represented by the slopes of linear regressions of ln(abundance) plotted against time, in years.
Change in abundance is a comparison of the mean of the earliest 5 years and the mean of the most recent 5 years in each time-series.
(1) Simon et al. 2002, (2) Kulka & Miri 2003a,b, (3) Siegstad et al. 2003a, (4) Murua 2003, (5) ICES 2003, (6) Kulka & Simpson 2002, (7) Hurlbut & Poirier 2001, (8) Bundy et al. 2001, (9) NFSC 2002, (10) Dorn et al. 1999, (11) Showell et al. 2003, (12) ICES 2004, (13) Heino et al. 2002, (14) Mohn et al. 2001, (15) Fanning et al. 2003, (16) Hunt et al. 2003, (17) Vázquez & Cerviño 2002, (18) Cerviño & Vázquez 2003, (19) Fréchet et al. 2003, (20) Lilly et al. 2003, (21) Healey et al. 2003, (22) Chouinard et al. 2003, (23) Brattey et al. 2003, (24) Clark & Hinze 2003, (25) O'Brien 1999, (26) Barot et al. 2004, (27) COSEWIC 2003, (28) Harris et al. 2002, (29) Frank et al. 2001, (30) Mohn & Simon 2002, (31) Hurley et al. 2003, (32) Van Eeckhaute et al. 2003, (33) Starr et al. 2002, (34) Sinclair et al. 2001, (35) Neilson et al. 1999, (36) Beanlands et al. 2000, (37) Kulka & Miri 2001, (38) Kulka & Miri 2003b, (39) Stanley et al. 2004, (40) Morin et al. 2001a, (41) Ávila de Melo et al. 2003, (42) Power 2003a, (43) Power 2003b, (44) Siegstad et al. 2003b, (45) Power 2001, (46) Kronlund et al. 2003, (47) Simpson & Kulka 2002, (48) Dwyer et al. 2003, (49) Morgan et al. 2003, (50) Alpoim 2003, (51) Morgan et al. 2002, (52) Morin et al. 2001b, (53) Fowler & Stobo 2000, (54) Morin & Bernier 2003, (55) Dwyer & Bowering 2003, (56) Darby et al. 2003, (57) Jørgensen 2003, (58) Darby 2003, (59) Grift et al. 2003, (60) Terceiro 2003, (61) Morin et al. 2002, (62) Parsons & Bowering 2003a, (63) Parsons & Bowering 2003b, (64) Bowering & Power 2002, (65) Swain & Poirier 2001, (66) Brodie et al. 2003, (67) Walsh & Morgan 1999, (68) Poirier & Morin 2002, (69) Stone & Legault 2003, (70) Cadrin & King 2003, (71) Cadrin 2003.
Research survey gear changed in this area in 1995, such that for stocks where comparisons of catchability between the gear were not done, time-series prior to and after the change are not comparable. As such, post-1992 slopes for these populations are the slope from 1995 onwards, and total change in abundance is undetermined.